Hearing LossNCT07303426
The Knowledge About the Underlying Cause of Hearing Loss in Children
An observational study of Hearing Loss, run by Karolinska Institutet at 1 site in Sweden.
Trial summary
This is a qualitative study to investigate children and their care-givers knowledge about the underlying aetiology of the childrens hearing loss. Both children and care-givers are given forms with questions about the type and level of hearing loss, if they know the cause and if it matters to them. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Hearing Loss
- How many people
- 156 participants
- Where
- 1 siteSweden
- Study dates
- 9 Sep 2024to 22 May 2025
- How long will I take part?
- 1 Day
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Children with hearing loss and their care-givers
Who may be able to join
- Children with Hearing loss and their care-givers
Who cannot join
- Children with no hearing loss or care-givers to children with no hearing loss.
Trial locations and contacts
1 site in 1 country.
About this study
This is a qualitative study to investigate children and their care-givers knowledge about the underlying aetiology of the childrens hearing loss. Both children and care-givers are given forms with questions about the type and level of hearing loss, if they know the cause and if it matters to them. This is to better understand the level of knowledge in both children and their care-givers about different causes of hearing loss. This will help to develop better clinical tools and routines of informing families about causal investigations in the future.
Read the detailed description
The knowledge of the aetiology in children with sensorineural hearing loss - does it matter?
Introduction In Sweden, hearing screening of newborns, preschoolers and school children can detect hearing loss (HL) early in life. The prevalence of HL in high income countries is 1-2/1000 at birth, increases to 3-4/1000 in school children and around 5/1000 in children aged 15-18. In the Stockholm region, all children with HL in need of intervention are enrolled at the Hearing Habilitation for children and youth at Karolinska university hospital where they are followed up until they finish high school.
As finding out that your child has a hearing loss hearing loss can be quite difficult to understand and accept for parents, the timepoint of diagnosis is not always the most appropriate time to offer investigations of the cause of the hearing loss. However, there are no clinical guidelines as when to offer it. During the succeeding regular follow-up visits of children with HL at the Hearing habilitation it is a common clinical experience that few children know why they have a HL and how it may change over their life course, and when they ask their parents, they do not know either. A reason for this may be that some parents were informed when their child was diagnosed years ago and chose not to investigate the cause. Another comment from parents, in cases where many years have passed since the diagnosis, is that some parents do not remember if they received a question about investigating the cause or not. This give rise to an ethical question from the child´s point of view; should the audiology doctor ask the parents if they want to investigate the cause of the HL again, or should they ask the child themselves? With age, children themselves may wonder: what is the cause of my HL and how will that affect my future? The knowledge and interest around the cause of the hearing loss is something that has not been investigated in a systematic manner before, but is important to provide the child with HL and their parents with the right support in the right time. As some etiologies affect other areas of development, knowing about the etiology of the hearing loss also gives professionals cues to provide the most optimal intervention. In this study, we want to examine what the caregivers of children as well as the children themselves know and how important they think it is to know about the cause of HL. Another motivation to pursue this study is that we do not know how many children in the intended target group who have investigated the etiology.
Scientific questions:
- Do caregivers and children with HL know the cause of the child's HL?
- What difference does knowing/not knowing about the cause of HL make for the children themselves and their parents?
- Do caregivers and children have different opinions about the importance of investigating the cause of HL?
Study design To collect data we will use a patient-related outcome measure (PROM) with questions specifically made for this study together with information around background variables. Information about the study and consent form will be mailed out to all children/youth enrolled at the Hearing Habilitation for Children and Youth born between 2010-2015 with diagnosis code H90.3 (bilateral sensorineural hearing loss) (n=327) and their guardians.
Procedures and materials
- Children with different types and degrees of HL born 2010-2015 and their parents enrolled at the Hearing Habilitation. Recruitment via letter home with information about the study, consent form and prepaid return envelope followed by a letter with a QR code/paper version.
- Children/families will be invited to complete a questionnaire (digital or/paper version) separately (questions about their knowledge about the cause of hearing loss) and a background form filled in by the child's parents (age, sex, type and degree of HL).
Clinical implications This project is one of the first to investigate this important, yet, challenging part of the intervention in children. In the Swedish healthcare system, children are supposed to seek help themselves from 13 years of age. As there is no systematically collected information on group level around the knowledge of the cause of hearing loss in this target group, the results from this study may contribute to a better understanding as to the importance of etiological diagnosis and surveillance of each child with HL. It will also act as a guidance to medical professionals and families to better understand the cause of HL and expectations of the child's hearing, speech and language development.
- Conditions
- Hearing Loss
- Keywords
- childhood hearing loss, questionnaires, hearing loss aetiology
- Medical subject headings
- Hearing Loss
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Group A | Consists of children with bilateral sensorineural hearing loss and their care-givers | |
| Group B | Consists of both children and care-givers who answer forms anonymously. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Do caregivers and children with HL know the cause of the child's HL
To study weather children and care-givers know the cause of the childs HL if available.
Measured: from sept 2024 to may 2025
To investigate children´s and caregivers perspectives on the importance of knowing the cause of the child´s hearing loss through questionnaires.
Questionnaires were distrubuted wither through mail or QR code for the parents and children to respond.
Measured: Group A: Sept 2024 to Nov 2024, Group B: Jan 2025 to May 2025
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Dec 2025
- Study start9 Sep 2024
- Primary completion22 May 2025
- Study completion22 May 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hearing LossStudies of the same condition, open and under way.
- More trials run by Karolinska InstitutetThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 156 participants (actual)
- Target duration
- 1 Day
Sponsor and investigators
- Lead sponsor
- Karolinska Institutet
- Sponsor type
- University, hospital or other
- Collaborators
- Karolinska University Hospital
- Responsible party
- Principal investigator, Anna Persson, Karolinska Institutet
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07303426
- Sponsor's protocol ID
- 2024-03470-01
- Status last verified
- Dec 2025
- First submitted
- 5 Dec 2025
- Last updated
- 24 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: IPD is only for this study
Study at a glance
From the registry record, last updated by the sponsor on 24 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Knowledge About the Underlying Cause of Hearing Loss in Children
- ClinicalTrials.gov ID
- NCT07303426
- Acronym / sponsor ID
- 2024-03470-01
- Conditions
- Hearing Loss
- Keywords
- childhood hearing loss, questionnaires, hearing loss aetiology
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 156 participants (actual)
- Lead sponsor
- Karolinska InstitutetUniversity, hospital or other
- Collaborators
- Karolinska University Hospital
- Study start
- 9 Sep 2024 (actual)
- Primary completion
- 22 May 2025 (actual)
- Study completion
- 22 May 2025 (actual)
- First posted
- 24 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a qualitative study to investigate children and their care-givers knowledge about the underlying aetiology of the childrens hearing loss. Both children and care-givers are given forms with questions about the type and level of hearing loss, if they know the cause and if it matters to them. This is to better understand the level of knowledge in both children and their care-givers about different causes of hearing loss. This will help to develop better clinical tools and routines of informing families about causal investigations in the future.
Detailed description
The knowledge of the aetiology in children with sensorineural hearing loss - does it matter?
Introduction In Sweden, hearing screening of newborns, preschoolers and school children can detect hearing loss (HL) early in life. The prevalence of HL in high income countries is 1-2/1000 at birth, increases to 3-4/1000 in school children and around 5/1000 in children aged 15-18. In the Stockholm region, all children with HL in need of intervention are enrolled at the Hearing Habilitation for children and youth at Karolinska university hospital where they are followed up until they finish high school.
As finding out that your child has a hearing loss hearing loss can be quite difficult to understand and accept for parents, the timepoint of diagnosis is not always the most appropriate time to offer investigations of the cause of the hearing loss. However, there are no clinical guidelines as when to offer it. During the succeeding regular follow-up visits of children with HL at the Hearing habilitation it is a common clinical experience that few children know why they have a HL and how it may change over their life course, and when they ask their parents, they do not know either. A reason for this may be that some parents were informed when their child was diagnosed years ago and chose not to investigate the cause. Another comment from parents, in cases where many years have passed since the diagnosis, is that some parents do not remember if they received a question about investigating the cause or not. This give rise to an ethical question from the child´s point of view; should the audiology doctor ask the parents if they want to investigate the cause of the HL again, or should they ask the child themselves? With age, children themselves may wonder: what is the cause of my HL and how will that affect my future? The knowledge and interest around the cause of the hearing loss is something that has not been investigated in a systematic manner before, but is important to provide the child with HL and their parents with the right support in the right time. As some etiologies affect other areas of development, knowing about the etiology of the hearing loss also gives professionals cues to provide the most optimal intervention. In this study, we want to examine what the caregivers of children as well as the children themselves know and how important they think it is to know about the cause of HL. Another motivation to pursue this study is that we do not know how many children in the intended target group who have investigated the etiology.
Scientific questions:
- Do caregivers and children with HL know the cause of the child's HL?
- What difference does knowing/not knowing about the cause of HL make for the children themselves and their parents?
- Do caregivers and children have different opinions about the importance of investigating the cause of HL?
Study design To collect data we will use a patient-related outcome measure (PROM) with questions specifically made for this study together with information around background variables. Information about the study and consent form will be mailed out to all children/youth enrolled at the Hearing Habilitation for Children and Youth born between 2010-2015 with diagnosis code H90.3 (bilateral sensorineural hearing loss) (n=327) and their guardians.
Procedures and materials
- Children with different types and degrees of HL born 2010-2015 and their parents enrolled at the Hearing Habilitation. Recruitment via letter home with information about the study, consent form and prepaid return envelope followed by a letter with a QR code/paper version.
- Children/families will be invited to complete a questionnaire (digital or/paper version) separately (questions about their knowledge about the cause of hearing loss) and a background form filled in by the child's parents (age, sex, type and degree of HL).
Clinical implications This project is one of the first to investigate this important, yet, challenging part of the intervention in children. In the Swedish healthcare system, children are supposed to seek help themselves from 13 years of age. As there is no systematically collected information on group level around the knowledge of the cause of hearing loss in this target group, the results from this study may contribute to a better understanding as to the importance of etiological diagnosis and surveillance of each child with HL. It will also act as a guidance to medical professionals and families to better understand the cause of HL and expectations of the child's hearing, speech and language development.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 1 Day
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group A | – | –Consists of children with bilateral sensorineural hearing loss and their care-givers |
| Group B | – | –Consists of both children and care-givers who answer forms anonymously. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Children with hearing loss and their care-givers
Key inclusion criteria (1 listed)
- Children with Hearing loss and their care-givers
Key exclusion criteria (1 listed)
- Children with no hearing loss or care-givers to children with no hearing loss.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Do caregivers and children with HL know the cause of the child's HL
Time frame: from sept 2024 to may 2025
To study weather children and care-givers know the cause of the childs HL if available.
To investigate children´s and caregivers perspectives on the importance of knowing the cause of the child´s hearing loss through questionnaires.
Time frame: Group A: Sept 2024 to Nov 2024, Group B: Jan 2025 to May 2025
Questionnaires were distrubuted wither through mail or QR code for the parents and children to respond.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Dec 2025.
- Individual participant dataSharing planned: No. IPD is only for this study
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hearing Loss, run by Karolinska Institutet at 1 site in Sweden.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 24 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Do caregivers and children with HL know the cause of the child's HL (time frame: from sept 2024 to may 2025). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Dec 2025.